Drugs / F520

Trials 10 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 11 trial
Phase 1 NCT03657381 Mar 2019 → Feb 2021 Hodgkin's lymphoma, lymphocytic depletion Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 1/21 trial
Phase 1/2 NCT05740215 May 2022 → May 2024 cancer Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 26 trials
Phase 2 NCT05741021 Mar 2023 → Oct 2024 non-small cell lung carcinoma Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 2 NCT05178836 Jan 2022 → Dec 2023 relapsed/refractory diffuse large B-cell lymphoma Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 2 NCT06226350 Mar 2021 → Dec 2023 cervical cancer Shandong New Time Pharmaceutical Co., LTD Completed No outcome recorded
Phase 2 NCT04636515 Jan 2021 → Mar 2022 urothelial carcinoma Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 2 NCT04457830 Nov 2020 → Jul 2022 peripheral T-cell lymphoma, not otherwise specified Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 2 NCT04457869 Nov 2020 → Jul 2022 central nervous system non-hodgkin lymphoma Shandong New Time Pharmaceutical Co., LTD Unknown No outcome recorded
Phase 2/32 trials
Phase 2/3 NCT06755515 Sep 2024 → Sep 2028 expected cervical cancer Shandong New Time Pharmaceutical Co., LTD Enrolling by invitation No outcome recorded
Phase 2/3 NCT05408221 Nov 2022 → Aug 2025 overdue hepatocellular carcinoma Shandong New Time Pharmaceutical Co., LTD Recruiting No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 10 sources stand behind the page.

FieldValueCited text
Known as F520 F520,IV, 3mg/kg every 3 weeks, for up to 2 years until disease progression, intolerable toxic reactions, or termination of treatment for other reasons.” NCT06226350
7

“Recombinant Programmed death-1(PD-1) humanized monoclonal antibody injection (company code: F520)” NCT03657381

NCT04457830

NCT05178836

NCT04636515

NCT05740215

NCT05741021

NCT04457869

Known as Rulonilimab ClinicalTrials.gov intervention name — accepted as the source's own label NCT05408221
1

NCT06755515

Action Inhibit “prevents binding of PD-1 with programmed death ligands 1 (PD-L1) and 2 (PD-L2)” NCT05178836
Modality Monoclonal antibody “humanized monoclonal antibodyNCT03657381
Route Intravenous “F520 (200mg) administered intravenously (IV) on Day 2 of each 14-day cycle for cycle 1.” NCT05178836